A case report of massive pulmonary tuberculosis and newly diagnosed systemic lupus erythematosus with complications

Key Clinical Message The diagnosis of extensive pulmonary tuberculosis, especially in young people, should take into account the possibility of an associated systemic autoimmune disease. Infections remain an important cause of morbidity and mortalityin systemic lupus erythematosus. This case illustrates the importance of recognizing the association of systemic autoimmune diseases and infections and the need for a multidisciplinary approach.


| INTRODUCTION
Although there has been significant improvement in outcome and survival in systemic lupus erythematosus (SLE), infections remain an important cause of morbidity and mortality. 1They can appear in the early or late stages of SLE, and account for about 14%-50% of hospitalizations. 2,3he increased risk of infections is attributed to diseaserelated factors that lead to dysregulation of the immune system and the use of immunosuppressive drugs. 4About half of patients with SLE experience a serious infection during the course of the disease, and 11%-23% of hospitalizations among patients with SLE are due to infections. 5 One-third of SLE-related deaths can be attributed to an infectious organism. 6,7The World Health Organization (WHO) Global Tuberculosis Report 2022 estimates 10.6 million new tuberculosis (TB) cases in 2021, most common in Southeast Asia (45%), Africa (23%), the Western Pacific (18%), and the Eastern Mediterranean (8.3%). 8here was a smaller share in America (2.9%), and Europe (2.2%). 8The estimated number of deaths from TB in the world is about 1.6 million, of which about 187,000 were human immunodeficiency virus (HIV) positive patients. 8he incidence of TB in patients with SLE is seven times higher than that in healthy populations in developed countries and is estimated at 5% in developing countries. 9

| CASE HISTORY/ EXAMINATION
A 22-year-old patient was hospitalized due to febrility, and a non-productive cough that had lasted for the past 9 months.He also noticed that he had poor effort tolerance, and in the last month had lost 10 kg of body weight.He was not on any drugs in chronic therapy.He did not drink alcohol nor smoke cigaretts.On admission, the patient was conscious, oriented, hypotensive (100/60 mmHg), subfebrile (37.4*C), acyanotic (Sp02: 92%) at room temperature, and of asthenic structure.The skin and visible mucous membranes were extremely pale, without rash.On auscultation breath sound intensity was reduced bilaterally was verified on both sides.Sinus tachycardia was noted in the electrocardiogram (ECG) record upon admission.On admission, laboratory findings showed anemia with elevated inflammatory parameters, and a liver lesion (Table 1).

DIAGNOSIS, INVESTIGATIONS AND TREATMENT)
A radiological image of the lungs was a completely changed.On the left side of the lungs completely changed architecture of the lung parenchyma with irregular, mostly oval transparencies dominantly in the upper and middle lung fields, and an air bronchogram in the lower lung field with spotty shadowing of the lung parenchyma basally is presented.On the right in the upper, partly in the middle lung field, inhomogeneous shadowing of the lung parenchyma with retraction of the horizontal interlobe and right hilus (Figure 1).
Immediately upon admission, sputum was analyzed for Mycobacterium tuberculosis (M.tb), which was directly positive (+++ [>100]), after which quadruple anti-tuberculosis therapy (ATT) (rifampin, isoniazid, pyrazinamide, and ethambutol) in a reduced dose according to body weight (body weight less than 50 kg) was included with gastroprotection, albumin replacement therapy, and preventive anticoagulant therapy with low molecular weight heparin, and continuous oxygen therapy with a flow rate of 4 L/min., and antipyretics.According to the current guidelines due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) epidemics, a PCR means polymerase chain reaction (PCR) test for SARS-CoV-2 was performed at the reception, which was positive, and the epidemiological measures, and symptomatic treatment was followed.After 14 days of hospitalization, a control test for SARS-CoV-2 was performed, which arrived negative.On the 10th day of hospitalization, the patient developed a rash on the skin, for which a dermatologist was consulted.ATT therapy was stopped and drugs were gradually introduced again.Pyrazinamide tablets were excluded from the therapy due to the suspicion that it caused skin allergy.Because of the massive pulmonary infiltrates, streptomycin (750 mg) intramuscularly was added for 2 months.The course of the disease was complicated on the 17th day of treatment when the patient experienced chest pain with recorded sinus tachycardia in the ECG, and due to suspected pulmonary embolisman urgent multislice computed tomography (MSCT) angiography F I G U R E 1 Chest X-ray on admission.
of the pulmonary arteries was performed, which showed "riding" and partial filling defects in the branches of the right pulmonary artery for the lower lung lobe (Figures 2  and 3).After confirming the diagnosis of pulmonary embolism, low molecular weight heparin in full therapeutic dose was included.Due to fever the infectologist was consulted.Enterococcus spp. was isolated in urine culture.In therapy, according to the antibiogram, intravenous linezolid was included.The control urine culture was negative.Due to the suspicion of an associated immunological diseases because of prolonged febrile state, swelling and joint pain, weight loss, and Raynaud's syndrome an immunologist was also consulted and recommended a complete immunological diagnostic processing.The markers for bloodtransmitted diseases arrived negative (Table 2).The SLICC Criteria for SLE were met for making the diagnosis of 10 One clinical criterion (arthritis) and four laboratory criteria were present (positive antibody to doublestranded deoxyribonucleic acid (antids-DNA), positive anticardiolipin antibodies, positive lupus anticoagulant (LAC), low C4, positive Coombs test in the absence of hemolytic anemia) (Table 3).The Sapporo criteria for the classification of the antiphospholipid syndrome (APS) were met. 11s part of the diagnostic recommendation by the immunologist, magnetic resonance imaging (MRI), and magnetic resonance angiogram (MRA) of the brain were also performed.The finding was unremarkable (Figures 4  and 5).In MRA using 3 DTOF techniques.The finding was unremarkable with an adequate course without clearly observed signs of aneurysm or other arteriovenous malformation (AVM) (Figures 6 and 7).

(OUTCOME AND FOLLOW-UP)
Based on the above, therapy for SLE was prescribed along with ATT therapy, which led to subjective and clinical improvement and a febrile state.The therapy for SLE was administered (decortine, azathioprine, and hydroxychloroquine).The patient gained 10 kg in body weight during his stay in the hospital.After 110 days of hospitalization, with the control sputum for M. Tuberculosis being negative, after the control x-ray of the lungs (Figure 8), showed improvement, the patient was discharged from the hospital.ATT therapy was conducted for 6 months (two months of the initiation phase, and the continuation phase for 4 months).Regular controls by a pulmonologist and immunologist were performed.

| DISCUSSION
There is a complex interaction between SLE and TB. 12,13atients with SLE have an increased risk of developing infections, including TB due to their impaired immune defence and use of immunosuppressive agents.In patients with SLE, TB is more likely to be extrapulmonary.Involvement is more severe, and relapses occur more often. 11Infections can also trigger autoimmune diseases and contribute to the induction and exacerbation of SLE. 12,14Diagnosing TB in patients with SLE is often a challenging task because they have many similar manifestations including fever, weight loss, and constitutional disturbances.In addition, pulmonary, and neurological manifestations can occur in both SLE and TB. 15 Therefore, common rheumatic diseases can be misdiagnosed as general infections, leading to a very high rate of misdiagnosis and underdiagnosis.Many exposed persons in endemic areas will be at risk of TB reactivation with autoimmune diseases or immunosuppressive drugs, so a multidisciplinary approach is needed to identify patients at increased risk of TB who will benefit from prophylactic therapy.

F I G U R E 2 T A B L E 2
MSCT-pulmonary angiography of the pulmonary arteries.F I G U R E 3 MSCT-pulmonary angiography of the pulmonary arteries.Laboratory of markers for blood transmitted disease findings.Negative (0,1) Anti HAV IgM + IgG Negative (2,46) Anti HBc /IgM + IgG Negative (2,41)

T A B L E 3 4 F I G U R E 5 F I G U R E 6
Laboratory of imunology findings.Magnetic resonance imaging (MRI) and magnetic resonance angiogram (MRA) of the brain.Magnetic resonance imaging (MRI) and magnetic resonance angiogram (MRA) of the brain.Magnetic resonance angiogram (MRA) using 3 D TOF techniques.